Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7578597 | 0.807 | 0.240 | 2 | 43505684 | missense variant | T/C | snv | 9.9E-02 | 0.14 | 2 | |
rs10203174 | 1.000 | 0.080 | 2 | 43462891 | intron variant | C/T | snv | 0.17 | 1 | ||
rs11899863 | 1.000 | 0.080 | 2 | 43391680 | intron variant | C/T | snv | 8.5E-02 | 1 |